{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Atlanta",
      "address_1": "400 Perimeter Center Ter Ne",
      "reason_for_recall": "Patient needs to be positioned as indicated by the treatment plan.",
      "address_2": "Ste 50",
      "product_quantity": "72",
      "code_info": "All versions of Monaco",
      "center_classification_date": "20130925",
      "distribution_pattern": "Distributed in Puerto Rico and the states of AK, AZ, CA, CO, CT, FL, IL, IN, MA, MD, MI, MN, MO, NC, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN, TX, VA, and  WA.",
      "state": "GA",
      "product_description": "Monaco RTP System Radiation Therapy Treatment Planning System.     Radiation treatment planning.",
      "report_date": "20131002",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Elekta, Inc.",
      "recall_number": "Z-2277-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65998",
      "termination_date": "20131223",
      "recall_initiation_date": "20130522",
      "postal_code": "30346-1227",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}